The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
126896761 12689676 1 I 20160804 20160812 20160826 20160826 EXP GB-MHRA-TPP36167998C4249803YC1470302468109 GB-SUN PHARMACEUTICAL INDUSTRIES LTD-2016RR-122352 RANBAXY 0.00 Y 0.00000 20160826 OT GB GB

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
126896761 12689676 1 PS Codeine CODEINE 1 Unknown U U 0
126896761 12689676 2 C AMOXICILLIN. AMOXICILLIN 1 Unknown 1 DF, DAILY 3 DF U U 0 1 DF
126896761 12689676 3 C ASPIRIN. ASPIRIN 1 Unknown 1 DF, DAILY 450 DF U U 0 1 DF
126896761 12689676 4 C PARACETAMOL ACETAMINOPHEN 1 Unknown 4 TIMES A DAY. U U 0 2 DF

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126896761 12689676 1 Product used for unknown indication
126896761 12689676 2 Product used for unknown indication
126896761 12689676 3 Product used for unknown indication
126896761 12689676 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126896761 12689676 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126896761 12689676 Rash

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
126896761 12689676 1 20160804 0
126896761 12689676 2 20160804 0
126896761 12689676 3 20150512 0
126896761 12689676 4 20150512 0